Functional Outcomes in COVID-19 Survivors and Use of a Digital Platform for Rehabilitation

COVID-19 Clinical Trial

Official title:

Functional Outcomes in COVID-19 Survivors and Use of a Digital Platform for Rehabilitation

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04695301
• Other study ID #: 34170820.0.1001.0071
• Status: Completed
• Phase: N/A
• Start date: July 1, 2020
• Est. completion date: October 1, 2021

Study information

• Verified date: July 2020
• Source: Hospital Israelita Albert Einstein
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

COVID-19, an acute respiratory disease caused by coronavirus-2 (SARS-CoV-2), and in most cases, causes mild to moderate symptoms of fever, cough and dyspnea. However, a not insignificant portion, given the total number of people affected, will present symptoms of severe acute respiratory failure and multiple organ failure, requiring hospitalization under intensive care, use of mechanical ventilation, prolonged period of immobilization and, consequently, physical, cognitive and psychological damage, which may affect survivors for a long period after hospitalization. All of these factors are known to have an impact on various areas of life: personal, social and economic, which makes the need for continued specific care after hospital discharge relevant. In this context, the role of rehabilitation programs is fundamental, aiming not only at a safer dehospitalization, but also at the continuity of care with the objective of restoring the biopsychosocial skills of these individuals, allowing functional independence for activities of daily life and a shorter return physical and social activities performed before the disease. However, the big challenge for the health system is how to offer this on a large scale. Therefore, knowing the clinical and functional profile of these patients at discharge and verifying the viability of a digital platform for rehabilitation and monitoring of these patients is the first step to allow the creation of a new form of continuity of care and access to affected patients with serious diseases such as COVID-19 and other syndromes capable of generate functional impairment. Therefore,the investigators objective is to characterize and monitor the functional profile and exercise capacity of patients affected by COVID-19 at the hospital discharge, as well as to verify the viability and compliance of patients to the use of a digital platform for the application of a distance rehabilitation program.

Description:

The investigators proposal is to characterize and evaluate the impact of the disease on the clinical, functional and social aspects in these patients affected by COVID-19 and to propose the continuity of specific care after hospital discharge with a physical rehabilitation program through a digital platform, remotely for a period of 3 months. The proposed hypothesis is that patients convalescing from COVID-19 and undergoing the rehabilitation program will have a gain in functional skills and quality of life. The professional team involved in this study will be responsible for managing, monitoring and evaluating the participating patients and monitoring the performance of the proposed functional exercises.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 25
• Est. completion date: October 1, 2021
• Est. primary completion date: July 1, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Men and women affected by COVID-19

• over 18 years of age, admitted to HIAE partner hospitals

Exclusion Criteria:

• presence of a physical or cognitive condition that makes it impossible or contraindicated to perform the 2-minute stride test and perform the proposed exercises.

• Patients with a more severe clinical and functional profile,

• Pregnant women

Related Conditions & MeSH terms

• Coronavirus Infections
• COVID-19
• Exercise Therapy

Intervention

Other:
• Rehabilitation protocol through a digital platform
During 3 months the patients will participate in a rehabilitation program through a digital platform

Locations

Country	Name	City	State
Brazil	Instituto Israelita de Ensino e Pesquisa Albert Einstein 's (IIEP)	São Paulo

Sponsors (1)

Lead Sponsor	Collaborator
Hospital Israelita Albert Einstein

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Characterize the clinical function profile of patients affected by COVID-19	Characterize the clinical functional profile of patients affected by COVID-19 by data from medical records	3 months
Primary	Characterize the exercise capacity of patients affected by COVID-19	Characterize the exercise capacity of patients affected by COVID-19 by 2-minute step test	3 months
Secondary	Assess clinical and demographic data	Assess clinical and demographic data	3 months
Secondary	Assess functional level at hospital discharge	Assess functional level at hospital discharge and 3 months after discharge by physical test	3 months
Secondary	Assess patient compliance of the rehabilitation program using the digital platform	Assess patient compliance of the rehabilitation program using the digital platform checking your adherence to the program	3 months